Author:
Li Xiaohong,Gao Xue,Huang Shasha,Han Mingyu,Kang Dongyang,Yang Jinyuan,Wu Xiedong,Zheng Qiuchen,Yuan Yongyi,Dai Pu,Wang Guojian
Funder
National Key Research and Development Program of China
National Natural Science Foundation of China
Natural Science Foundation of Hainan Province
Natural Science Foundation of Beijing Municipality
National Key Scientific Instrument and Equipment Development Projects of China
Subject
Cell Biology,Developmental Biology,General Medicine
Reference5 articles.
1. A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness;Waardenburg;Am. J. Hum. Genet.,1951
2. Review and update of mutations causing Waardenburg syndrome;Pingault;Hum. Mutat.,2010
3. Mobile DNA elements in the generation of diversity and complexity in the brain;Erwin;Nat. Rev. Neurosci.,2014
4. Yang, C., Li, Y., Trottier, M., et al. Insertion of an SVA element in MSH2 as a novel cause of Lynch syndrome. 2021 Aug;60(8):571-576. doi: 10.1002/gcc.22950. PubMed PMID: 33822432.
5. Klein, C., Capponi, S., Dissection of TAF1 neuronal splicing and implications for neurodegeneration in X-linked dystonia-parkinsonism. Annals of neurology. 2021;3(4):fcab253. doi: 10.1002/ana.2548810.1093/braincomms/fcab253. PubMed PMID: 34746789.
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献